{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "La Follette",
      "address_1": "1501 E Central Ave",
      "reason_for_recall": "The sterile packaging has the potential to be compromised.",
      "address_2": "",
      "product_quantity": "669 units",
      "code_info": "Catalog Number DP40K; Lot Numbers: 74F1802710, 74G1802678, 74H1800763, 74D1900657, 74C1900811, 74D1700564",
      "center_classification_date": "20200313",
      "distribution_pattern": "International distribution of Kuwait City, Kuwait.",
      "state": "TN",
      "product_description": "Teleflex Pilling Aortic Punch, 4.0mm.  Sterile, Rx Only, disposable. Included as part of Intl-Cardiac Surgery Kit - Product Usage: This device is used for cardiovascular surgical procedures.",
      "report_date": "20200325",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Deroyal Industries, Inc. Lafollette",
      "recall_number": "Z-1483-2020",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "84943",
      "termination_date": "20210211",
      "more_code_info": "",
      "recall_initiation_date": "20200206",
      "postal_code": "37766-2892",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}